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14470-28-1

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14470-28-1 Usage

Chemical Properties

PALE YELLOW TO YELLOW-BEIGE OR PINK CRYST. POWDER

Uses

Different sources of media describe the Uses of 14470-28-1 differently. You can refer to the following data:
1. 4-Methoxytriphenylmethyl chloride is used in the synthesis of N-sulfonyl imines.
2. It is used as selective protecting reagent that is used for primary hydroxyl groups.

Hazard

Skin and eye irritant.

Check Digit Verification of cas no

The CAS Registry Mumber 14470-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,7 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14470-28:
(7*1)+(6*4)+(5*4)+(4*7)+(3*0)+(2*2)+(1*8)=91
91 % 10 = 1
So 14470-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H17ClO/c1-22-19-14-12-18(13-15-19)20(21,16-8-4-2-5-9-16)17-10-6-3-7-11-17/h2-15H,1H3

14470-28-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail
  • TCI America

  • (M0790)  4-Methoxytrityl Chloride [Hydroxyl Protecting Agent]  >98.0%(HPLC)(T)

  • 14470-28-1

  • 25g

  • 660.00CNY

  • Detail
  • TCI America

  • (M0790)  4-Methoxytrityl Chloride [Hydroxyl Protecting Agent]  >98.0%(HPLC)(T)

  • 14470-28-1

  • 250g

  • 4,750.00CNY

  • Detail
  • Alfa Aesar

  • (A10545)  4-Methoxytrityl chloride, 97%   

  • 14470-28-1

  • 10g

  • 351.0CNY

  • Detail
  • Alfa Aesar

  • (A10545)  4-Methoxytrityl chloride, 97%   

  • 14470-28-1

  • 50g

  • 1294.0CNY

  • Detail
  • Alfa Aesar

  • (A10545)  4-Methoxytrityl chloride, 97%   

  • 14470-28-1

  • 250g

  • 5944.0CNY

  • Detail
  • Aldrich

  • (129208)  4-Methoxytriphenylmethylchloride  97%

  • 14470-28-1

  • 129208-5G

  • 299.52CNY

  • Detail
  • Aldrich

  • (129208)  4-Methoxytriphenylmethylchloride  97%

  • 14470-28-1

  • 129208-25G

  • 1,105.65CNY

  • Detail
  • Aldrich

  • (129208)  4-Methoxytriphenylmethylchloride  97%

  • 14470-28-1

  • 129208-100G

  • 3,223.35CNY

  • Detail

14470-28-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methoxytriphenylchloromethane

1.2 Other means of identification

Product number -
Other names 4-Monomethoxytrityl chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14470-28-1 SDS

14470-28-1Synthetic route

p-methoxytrityl alcohol
847-83-6

p-methoxytrityl alcohol

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
With acetyl chloride In benzene for 1h; Heating;89%
With hydrogenchloride In toluene at 15 - 30℃; Solvent; Temperature;89.1%
With acetyl chloride In benzene at 80℃; for 0.5h; Reflux;67%
benzophenone
119-61-9

benzophenone

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1) Mg / 1) ether, 2) benzene
2: 89 percent / acetyl chloride / benzene / 1 h / Heating
View Scheme
Multi-step reaction with 2 steps
1: benzene; diethyl ether
2: benzene
View Scheme
Multi-step reaction with 2 steps
1.1: magnesium / diethyl ether / 2 h / 35 °C
1.2: 24 h / Reflux
2.1: acetyl chloride / benzene / Reflux
View Scheme
Multi-step reaction with 2 steps
1.1: magnesium / diethyl ether / 2 h / 35 °C
1.2: 24 h / Reflux
2.1: acetyl chloride / benzene / 0.75 h / Reflux
View Scheme
Multi-step reaction with 2 steps
1: magnesium / tetrahydrofuran / 24 h / 60 °C / Schlenk technique; Inert atmosphere
2: acetyl chloride / benzene / 0.5 h / 80 °C / Reflux
View Scheme
1-bromo-4-methoxy-benzene
104-92-7

1-bromo-4-methoxy-benzene

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1) Mg / 1) ether, 2) benzene
2: 89 percent / acetyl chloride / benzene / 1 h / Heating
View Scheme
Multi-step reaction with 2 steps
1.1: magnesium / diethyl ether / 2 h / 35 °C
1.2: 24 h / Reflux
2.1: acetyl chloride / benzene / Reflux
View Scheme
Multi-step reaction with 2 steps
1.1: magnesium / diethyl ether / 2 h / 35 °C
1.2: 24 h / Reflux
2.1: acetyl chloride / benzene / 0.75 h / Reflux
View Scheme
Multi-step reaction with 2 steps
1: magnesium / tetrahydrofuran / 24 h / 60 °C / Schlenk technique; Inert atmosphere
2: acetyl chloride / benzene / 0.5 h / 80 °C / Reflux
View Scheme
p-methoxytrityl alcohol
847-83-6

p-methoxytrityl alcohol

acetyl chloride
75-36-5

acetyl chloride

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
With benzene
With diethyl ether
p-hydroxytrityl alcohol
15658-11-4

p-hydroxytrityl alcohol

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: NaOH-solution
2: diethyl ether
View Scheme
4-methoxyphenyl magnesium bromide
13139-86-1

4-methoxyphenyl magnesium bromide

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: benzene; diethyl ether
2: benzene
View Scheme
4-Methoxybenzophenone
611-94-9

4-Methoxybenzophenone

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: magnesium
1.2: diethyl ether / 1 h / Heating
2.1: thionyl chloride / CCl4 / 5 h / 20 °C
View Scheme
bromobenzene
108-86-1

bromobenzene

(hexacarbonyl)chromium

(hexacarbonyl)chromium

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: magnesium
1.2: diethyl ether / 1 h / Heating
2.1: thionyl chloride / CCl4 / 5 h / 20 °C
View Scheme
etheric 4-methoxy-triphenyl-carbinol solution

etheric 4-methoxy-triphenyl-carbinol solution

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
With hydrogenchloride
Dichlorodiphenylmethane
2051-90-3

Dichlorodiphenylmethane

methoxybenzene
100-66-3

methoxybenzene

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

Conditions
ConditionsYield
With carbon disulfide; aluminium trichloride
hydrogenchloride
7647-01-0

hydrogenchloride

1,2-bis-(4-methoxy-phenyl)-1,1,2,2-tetraphenyl-ethane
860734-05-0

1,2-bis-(4-methoxy-phenyl)-1,1,2,2-tetraphenyl-ethane

benzene
71-43-2

benzene

A

1-(4-methoxyphenyl)diphenylmethane
13865-56-0

1-(4-methoxyphenyl)diphenylmethane

B

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

methyl 3-azido-3-deoxy-α-D-arabinofuranoside
66108-04-1

methyl 3-azido-3-deoxy-α-D-arabinofuranoside

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

methyl-3-deoxy-3-azido-5-O-para-monomethoxytrityl-α-D-arabinofuranose
153206-09-8

methyl-3-deoxy-3-azido-5-O-para-monomethoxytrityl-α-D-arabinofuranose

Conditions
ConditionsYield
With pyridine for 17h; Ambient temperature;100%
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

5-Fluoro-2'-deoxyuridine
50-91-9

5-Fluoro-2'-deoxyuridine

5'-O-(4-monomethoxytrityl)-2'-deoxy-5-fluorouridine
103767-37-9

5'-O-(4-monomethoxytrityl)-2'-deoxy-5-fluorouridine

Conditions
ConditionsYield
With pyridine for 48h; Ambient temperature;100%
With pyridine at 20℃; for 5h;94%
In pyridine for 24h; Ambient temperature;86%
(2Z,4E,10E,12E)-(6R,7S,8S,14S,15R,16S)-7-(Diethyl-isopropyl-silanyloxy)-15,17-dihydroxy-2,14-dimethoxy-4,6,8,10,16-pentamethyl-heptadeca-2,4,10,12-tetraenoic acid methyl ester
188938-33-2

(2Z,4E,10E,12E)-(6R,7S,8S,14S,15R,16S)-7-(Diethyl-isopropyl-silanyloxy)-15,17-dihydroxy-2,14-dimethoxy-4,6,8,10,16-pentamethyl-heptadeca-2,4,10,12-tetraenoic acid methyl ester

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

(2Z,4E,10E,12E)-(6R,7S,8S,14S,15R,16S)-7-(Diethyl-isopropyl-silanyloxy)-15-hydroxy-2,14-dimethoxy-17-[(4-methoxy-phenyl)-diphenyl-methoxy]-4,6,8,10,16-pentamethyl-heptadeca-2,4,10,12-tetraenoic acid methyl ester
188938-34-3

(2Z,4E,10E,12E)-(6R,7S,8S,14S,15R,16S)-7-(Diethyl-isopropyl-silanyloxy)-15-hydroxy-2,14-dimethoxy-17-[(4-methoxy-phenyl)-diphenyl-methoxy]-4,6,8,10,16-pentamethyl-heptadeca-2,4,10,12-tetraenoic acid methyl ester

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 3.5h; Ambient temperature;100%
With triethylamine In dichloromethane at 25℃; for 5h;91%
({(2-Amino-ethyl)-[2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-methyl)-phosphonic acid bis-[2-(4-nitro-phenyl)-ethyl] ester
202914-69-0

({(2-Amino-ethyl)-[2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-methyl)-phosphonic acid bis-[2-(4-nitro-phenyl)-ethyl] ester

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

({(2-{[(4-Methoxy-phenyl)-diphenyl-methyl]-amino}-ethyl)-[2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-methyl)-phosphonic acid bis-[2-(4-nitro-phenyl)-ethyl] ester
202914-62-3

({(2-{[(4-Methoxy-phenyl)-diphenyl-methyl]-amino}-ethyl)-[2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetyl]-amino}-methyl)-phosphonic acid bis-[2-(4-nitro-phenyl)-ethyl] ester

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine at 0 - 5℃; for 12h;100%
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

(2Z,4E,12E,14E)-(6R,7R,8S,9S,10R,16S,17R,18S)-7,9-Bis-(diethyl-isopropyl-silanyloxy)-8-ethyl-17,19-dihydroxy-2,16-dimethoxy-4,6,10,12,18-pentamethyl-nonadeca-2,4,12,14-tetraenoic acid methyl ester
213408-82-3

(2Z,4E,12E,14E)-(6R,7R,8S,9S,10R,16S,17R,18S)-7,9-Bis-(diethyl-isopropyl-silanyloxy)-8-ethyl-17,19-dihydroxy-2,16-dimethoxy-4,6,10,12,18-pentamethyl-nonadeca-2,4,12,14-tetraenoic acid methyl ester

(2Z,4E,12E,14E)-(6R,7R,8S,9S,10R,16S,17R,18S)-7,9-Bis-(diethyl-isopropyl-silanyloxy)-8-ethyl-17-hydroxy-2,16-dimethoxy-19-[(4-methoxy-phenyl)-diphenyl-methoxy]-4,6,10,12,18-pentamethyl-nonadeca-2,4,12,14-tetraenoic acid methyl ester
213408-83-4

(2Z,4E,12E,14E)-(6R,7R,8S,9S,10R,16S,17R,18S)-7,9-Bis-(diethyl-isopropyl-silanyloxy)-8-ethyl-17-hydroxy-2,16-dimethoxy-19-[(4-methoxy-phenyl)-diphenyl-methoxy]-4,6,10,12,18-pentamethyl-nonadeca-2,4,12,14-tetraenoic acid methyl ester

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane at 25℃; for 3h;100%
With dmap; triethylamine In dichloromethane for 3h; Ambient temperature;
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

(3S)-4-phenylsulfonyl-2,3-dihydrofuran-3-methanol
287933-70-4

(3S)-4-phenylsulfonyl-2,3-dihydrofuran-3-methanol

(3R)-3-(((4-methoxyphenyl)-diphenylmethoxy)-methyl)-4-phenylsulfonyl-2,3-dihydrofuran
287933-90-8

(3R)-3-(((4-methoxyphenyl)-diphenylmethoxy)-methyl)-4-phenylsulfonyl-2,3-dihydrofuran

Conditions
ConditionsYield
With dmap; triethylamine Alkylation;100%
With dmap; triethylamine In dichloromethane at 20℃; for 2h;100%
2',3'-O-isopropylideneinosine
2140-11-6

2',3'-O-isopropylideneinosine

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

5'-O-(monomethoxytrityl)-2',3'-O-isopropylideneinosine
239080-20-7

5'-O-(monomethoxytrityl)-2',3'-O-isopropylideneinosine

Conditions
ConditionsYield
In pyridine at 20℃; for 40h; Alkylation;100%
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

(1R,2S)-1-[(2R,3S)-3-(tert-Butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-2-methyl-propane-1,3-diol
349552-49-4

(1R,2S)-1-[(2R,3S)-3-(tert-Butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-2-methyl-propane-1,3-diol

(1R,2S)-1-[(2R,3S)-3-(tert-Butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-3-[(4-methoxy-phenyl)-diphenyl-methoxy]-2-methyl-propan-1-ol
349552-50-7

(1R,2S)-1-[(2R,3S)-3-(tert-Butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-3-[(4-methoxy-phenyl)-diphenyl-methoxy]-2-methyl-propan-1-ol

Conditions
ConditionsYield
With pyridine; dmap In dichloromethane at 23℃; for 2.7h;100%
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

(2R,3S,5R,6S)-2-Hydroxymethyl-5-triisopropylsilanyloxy-6-vinyl-tetrahydro-pyran-3-ol
370886-82-1

(2R,3S,5R,6S)-2-Hydroxymethyl-5-triisopropylsilanyloxy-6-vinyl-tetrahydro-pyran-3-ol

(2R,3S,5R,6S)-2-[(4-Methoxy-phenyl)-diphenyl-methoxymethyl]-5-triisopropylsilanyloxy-6-vinyl-tetrahydro-pyran-3-ol
370886-66-1

(2R,3S,5R,6S)-2-[(4-Methoxy-phenyl)-diphenyl-methoxymethyl]-5-triisopropylsilanyloxy-6-vinyl-tetrahydro-pyran-3-ol

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane at 20℃;100%
3-bromopropylamine hydrochloride
5003-71-4

3-bromopropylamine hydrochloride

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

N-(4-monomethoxytrityl)-3-bromopropylamine
501097-15-0

N-(4-monomethoxytrityl)-3-bromopropylamine

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 23℃;100%
With TEA In dichloromethane at 20℃; for 0h;95%
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

(2Z,5Z)-8-[(2S,4S,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxymethyl)-tetrahydro-furan-2-yl]-6-chloro-2-methyl-octa-2,5-dien-1-ol
516457-60-6

(2Z,5Z)-8-[(2S,4S,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxymethyl)-tetrahydro-furan-2-yl]-6-chloro-2-methyl-octa-2,5-dien-1-ol

tert-Butyl-[(2S,3S,5S)-5-{(3Z,6Z)-3-chloro-8-[(4-methoxy-phenyl)-diphenyl-methoxy]-7-methyl-octa-3,6-dienyl}-2-(4-methoxy-benzyloxymethyl)-tetrahydro-furan-3-yloxy]-dimethyl-silane
516457-75-3

tert-Butyl-[(2S,3S,5S)-5-{(3Z,6Z)-3-chloro-8-[(4-methoxy-phenyl)-diphenyl-methoxy]-7-methyl-octa-3,6-dienyl}-2-(4-methoxy-benzyloxymethyl)-tetrahydro-furan-3-yloxy]-dimethyl-silane

Conditions
ConditionsYield
In pyridine100%
methyl 6-aminocaproate hydrochloride
1926-80-3

methyl 6-aminocaproate hydrochloride

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

6-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-hexanoic acid methyl ester
766548-72-5

6-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-hexanoic acid methyl ester

Conditions
ConditionsYield
With TEA In dichloromethane100%
1-{2'-[(tert-butyl)dimethylsilyloxy]-4'-hydroxycyclohexyl}uracil
878550-04-0

1-{2'-[(tert-butyl)dimethylsilyloxy]-4'-hydroxycyclohexyl}uracil

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

1-{2'-[(tert-butyl)dimethylsilyloxy]-4'-[(4-methoxyphenyl)diphenylmethoxy]cyclohexyl}uracil
878550-06-2

1-{2'-[(tert-butyl)dimethylsilyloxy]-4'-[(4-methoxyphenyl)diphenylmethoxy]cyclohexyl}uracil

Conditions
ConditionsYield
With pyridine100%
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

C67H67NO15
159858-20-5

C67H67NO15

Conditions
ConditionsYield
With pyridine In dichloromethane100%
C8H14O5
930807-83-3

C8H14O5

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

C28H30O6
930807-84-4

C28H30O6

Conditions
ConditionsYield
With pyridine; dmap In dichloromethane at 20℃; for 1h;100%
N-1-(4'-seleno-β-D-ribofuranosyl)-thymine
1030021-66-9

N-1-(4'-seleno-β-D-ribofuranosyl)-thymine

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

5-methyl-5'-O-monomethoxytrityl-4'-selenouridine

5-methyl-5'-O-monomethoxytrityl-4'-selenouridine

Conditions
ConditionsYield
With dmap In pyridine at 20℃;100%
(R)-3-(p-methoxyphenoxy)-1,2-propanediol
17131-52-1, 124933-35-3, 131064-88-5, 131064-87-4

(R)-3-(p-methoxyphenoxy)-1,2-propanediol

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

C30H30O5
955948-40-0

C30H30O5

Conditions
ConditionsYield
With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 1h;100%
With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 2h;88%
C23H28N2O8

C23H28N2O8

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

C43H44N2O9

C43H44N2O9

Conditions
ConditionsYield
With pyridine at 0 - 20℃; Inert atmosphere;100%
With pyridine at 0 - 20℃; Inert atmosphere;
With pyridine at 0 - 20℃; Inert atmosphere;
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

thymidine
50-89-5

thymidine

5'-O-(4-monomethoxytrityl)-2'-deoxythymidine
42926-80-7

5'-O-(4-monomethoxytrityl)-2'-deoxythymidine

Conditions
ConditionsYield
With dmap; triethylamine In N,N-dimethyl-formamide at 20℃; for 3.5h;99%
With dmap; triethylamine In N,N-dimethyl-formamide at 20℃; for 4h; Inert atmosphere;97%
With pyridine94%
ethyl N-(2-aminoethyl)glycinate dihydrochloride

ethyl N-(2-aminoethyl)glycinate dihydrochloride

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

(2-{[(4-Methoxy-phenyl)-diphenyl-methyl]-amino}-ethylamino)-acetic acid ethyl ester
178389-68-9

(2-{[(4-Methoxy-phenyl)-diphenyl-methyl]-amino}-ethylamino)-acetic acid ethyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; for 1h;99%
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

3'-deoxy-3'-C-(iodomethyl)-2'-O-(2-methoxyethyl)-5-methyluridine
312934-35-3

3'-deoxy-3'-C-(iodomethyl)-2'-O-(2-methoxyethyl)-5-methyluridine

3'-deoxy-3'-C-(iodomethyl)-2'-O-(2-methoxyethyl)-5'-O-(4-methoxytrityl)-5-methyluridine
312934-48-8

3'-deoxy-3'-C-(iodomethyl)-2'-O-(2-methoxyethyl)-5'-O-(4-methoxytrityl)-5-methyluridine

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran; ethyl acetate at 20℃;99%
Etherification;
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran; ethyl acetate at 20℃; for 48h;
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran; ethyl acetate
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran; ethyl acetate at 20℃; for 48h;690 mg
2'-deoxyuridine
951-78-0

2'-deoxyuridine

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

O5'-trityl-2'-deoxy-uridine
14270-73-6

O5'-trityl-2'-deoxy-uridine

Conditions
ConditionsYield
With pyridine for 2h; Heating / reflux;99%
2'-deoxyuridine
951-78-0

2'-deoxyuridine

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

1-{4-hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydrofuran-2-yl}-1H-pyrimidine-2,4-dione
70255-96-8

1-{4-hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydrofuran-2-yl}-1H-pyrimidine-2,4-dione

Conditions
ConditionsYield
With pyridine for 2h; Heating;99%
With pyridine; dmap at 50℃; for 40h; Inert atmosphere;69%
(S)-1-O-(4-methoxyphenyl)glycerol
17131-52-1, 124933-35-3, 131064-87-4, 131064-88-5

(S)-1-O-(4-methoxyphenyl)glycerol

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

C30H30O5
955948-67-1

C30H30O5

Conditions
ConditionsYield
With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 1h;99%
With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 2h;91%
5-(3-bromo-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine
1262858-69-4

5-(3-bromo-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

(RS)-[bis-(4-methoxy-phenyl)-phenyl-methyl]-[5-(3-bromo-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-amine
1266784-96-6

(RS)-[bis-(4-methoxy-phenyl)-phenyl-methyl]-[5-(3-bromo-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-amine

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;99%
mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

N-Methyl-1,3-propanediamine
6291-84-5

N-Methyl-1,3-propanediamine

C24H28N2O
1599485-90-1

C24H28N2O

Conditions
ConditionsYield
In diethyl ether; dichloromethane for 2h;99%
C19H19ClN8O4

C19H19ClN8O4

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

C39H35ClN8O5

C39H35ClN8O5

Conditions
ConditionsYield
With dmap; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 16h; Reagent/catalyst; Inert atmosphere;98.51%
ethanolamine
141-43-5

ethanolamine

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

2-(((4-methoxyphenyl)diphenylmethyl)amino)ethanol
113019-11-7

2-(((4-methoxyphenyl)diphenylmethyl)amino)ethanol

Conditions
ConditionsYield
With pyridine; triethylamine at 20℃; for 1h;98%
With pyridine; triethylamine at 20℃; for 1h;98%
With pyridine; triethylamine at 20℃; for 1h;98%
Inosine
58-63-9

Inosine

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

5'-O-(4-methoxytrityl)inosine
69659-63-8

5'-O-(4-methoxytrityl)inosine

Conditions
ConditionsYield
With pyridine In dimethyl sulfoxide for 19h;98%
N4-benzoylcytidine
13089-48-0

N4-benzoylcytidine

mono-4-methoxytrityl chloride
14470-28-1

mono-4-methoxytrityl chloride

N4-benzoyl-5'-O-(4-monomethoxytrityl)cytidine
72409-15-5

N4-benzoyl-5'-O-(4-monomethoxytrityl)cytidine

Conditions
ConditionsYield
In pyridine; dimethyl sulfoxide for 24h; Ambient temperature;98%
With pyridine at 20℃; for 18h;82%

14470-28-1Relevant articles and documents

Modified aminoacyl-tRNA. 3. A general procedure for the synthesis of dipeptidyl transfer RNA.

Lapidot,de Groot,Rappoport,Hamburger

, p. 532 - 539 (1967)

-

White,Stout

, p. 2915 (1962)

A simple 4 - methoxy trityl chloride preparation process

-

Paragraph 0030-0040, (2019/06/05)

The invention discloses a simple 4 - methoxy trityl chloride preparation process, firstly the MMT - OH 290 g, reaction solvent 900 - 1000 g into the reaction bottle in four, lowering the temperature to 15 °C, opening stirring; through hydrogen chloride, in touch with the reaction temperature is 25 - 30 °C; in touch with the process, TLC monitoring reaction process; complete reaction of the raw materials, the amount of hydrogen chloride is 50 - 55 g; reaction solution is 40 - 65 °C concentrated under reduced pressure, adding [...] 350 g, lowering the temperature to 10 - 25 °C; thermal insulation stirring 1 h, vacuum filtration, the filter cake is petroleum ether 100 ml leaching a; infrared lamp 50 - 55 °C drying, getting white crystal 265 - 275 g, yield 85.8 - 89.1%, HPLC purity 98% or more, the invention relates to hydrogen chloride as the MMT - Cl of chlorine, and is simple, three waste is greatly reduced, the overall process is simple, after treatment is convenient, and good product quality, low cost, and improves the product competitiveness.

METHOD OF INHIBITING APOLIPOPROTEIN-E EXPRESSION COMPRISING ADMINISTERING A TRIARYLMETHYL AMINE COMPOUND

-

Paragraph 0049, (2014/02/15)

This invention offers an effective method of inhibiting the expression of apolipoprotein E by mammalian cells. Apolipoprotein E is a protein that plays a significant role in the development of Alzheimer's Disease in humans. The method comprises administering an effective amount of a triarylmethyl amine compound having the general formula: wherein the R1 group may comprise acyclic amines and aliphatic amines. The R2 group may comprise one of three aryl varieties: aryl, substituted aryl, or heterocycle. Triarylamine compounds inhibit apolipoprotein E expression in mammalian cells. In one aspect of the invention the mammalian cells may be human cells, and more specifically may be human brain cells.

Base-induced rearrangement of tritylamines to imines: discovery and investigation of the mechanism

Theodorou, Vassiliki,Skobridis, Konstantinos,Karkatsoulis, Aris

, p. 4284 - 4289 (2007/10/03)

An unexpected compound, the aniline derived benzophenone imine, was isolated when tritylamine was treated with n-BuLi and alkyl halides, during the formation of N-alkyl tritylamines, in the process of preparing primary amines. A nucleophilic attack of the nitrogen anion of tritylamide on the adjacent C-bonded phenyl, either substituted or not, involving a bridging anionic intermediate, is proposed for this base-induced tritylamine rearrangement to produce the corresponding imine. Electron-withdrawing groups in the aromatic ring, favoring the negative charge development, affect the relative migratory tendencies.

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